Ning Wang1,2
Hongyu Yi1Liang Fang1Jingyi Jin1Qianli Ma1Yuting Shen1Juan Li1Shuang Liang1Jie Xiong1Zhuo Li1Hanyu Zeng1Fengliang Jiang2Boquan Jin1
Lihua Chen1*- 1Department of Immunology, The Fourth Military Medical University, Xi'an, China
- 2Department of Immunology, Xi'an Medical University, Xi'an, China
Cluster of differentiation 226 (CD226) molecules play a crucial role in the activation of effector CD4+ T cells during the immune response process, but a cell-intrinsic function of CD226 in CD4+ T subsets is not clear. In this study, we showed that Cd226−/− mice were resistant to myelin oligodendrocyte glycoprotein peptide 35-55 (MOG35−55)-induced experimental autoimmune encephalomyelitis (EAE) with highly expressed IL-10+CD4+ T cells and downregulated IL-17A+CD4+ T cells when compared with wild-type (WT) mice. Th17 cell infiltration into the central nervous system (CNS) was largely decreased in the absence of CD226 during EAE. CD226 deficiency facilitated the proliferation of regulatory T cells (Tregs), with increased numbers of Tregs observed in EAE mice, and supported the elevated induced regulatory T cell (iTregs) proliferation in vitro. The Akt and Erk signaling pathways were shown to be involved in Cd226−/− Treg proliferation and function in vivo and in vitro. These findings collectively indicate that CD226 is a key molecule regulating the Treg-mediated suppression of autoimmune responses by inhibiting Treg proliferation. Thus, the results of this study identify additional mechanisms by which CD226 regulates Treg functions in EAE and supports the potential therapeutic effects of anti-CD226 molecules on autoimmune diseases.
Introduction
Cluster of differentiation 226 (CD226) is an adhesion molecule belonging to the immunoglobulin superfamily (1) that is ubiquitously and constitutively expressed on the majority of natural killer (NK) cells, T cells, and other immune cells and competes with the immunoreceptor tyrosine inhibition motif domain (TIGIT) for binding to the ligands CD155 and CD112 (2). Previous studies have reported that CD226 triggers the effector function of NK cells and contributes to Lymphocyte Function-associated Antigen (LFA)-1 signaling that promotes T cell activation (3). As an adhesion molecule, CD226 mediates cellular adhesion during pathological inflammation, and accumulating reports have shown that CD226 is associated with several autoimmune diseases (4, 5). Moreover, CD226 has been identified as an autoimmune susceptibility gene, and its allelic variants are linked to the development of multiple sclerosis (MS), systemic lupus erythaematosus (SLE), rheumatoid arthritis (RA), and juvenile idiopathic arthritis (JIA) (6, 7). Additionally, CD226 has also been demonstrated to be involved in the pathogenesis of autoimmune diseases by promoting self-reactive CD4+ T cell activation (8, 9) and triggering naïve CD4+ T cell differentiation and proliferation (3). Although the role of CD226 in autoimmune diseases has been well-documented, the molecular mechanisms associated with CD226 activity in these diseases are not clear.
MS is a chronic demyelinating autoimmune disease of the central nervous system (CNS) that is primarily mediated by T lymphocytes and is characterized by widespread inflammatory processes in the CNS, immune dysregulation, and immune over-activity. However, there are limited effective treatment solutions for this disease (10). The experimental autoimmune encephalomyelitis (EAE) model is one of the most suitable models for studying the pathogenesis of MS (11). Studies have shown that CD4+ T cells from T cell receptor (TCR) transgenic mice engineered to express TCR-specific myelin oligodendrocyte glycoprotein peptide 35-55 (MOG35−55) develop CNS inflammation, suggesting that CD4+ T cells play a central role in EAE (12). Previous studies have shown that excessive activation of auto-reactive CD4+ T cells, especially helper T (Th) 17 cells and the weakened function of regulatory T cells (Tregs) facilitates the development and advancement of MS (13). Although some studies have preliminarily confirmed that the reduction of the suppressive capabilities and the altered molecular expression of Tregs is linked to the pathogenesis of MS, the exact mechanism of auto-reactive CD4+ T cell dysregulation remains unclear (14, 15).
Tregs are characterized by the expression of transcription factor Foxp3 and play a crucial role in maintaining peripheral immune tolerance during autoimmune disease (16). Many investigations have reported that Tregs inhibit autoimmune responses by suppressing the effector CD4+ T cell (Teff) subsets (17). Under the appropriate conditions, such as a specific cytokine environment, Tregs inhibit Th17 cell differentiation via repression of the transcription factor RORγt (18). However, under inflammatory conditions, some Tregs may lose Foxp3 expression and lineage stability, which may contribute to uncontrolled inflammation (19). It has been reported that CD226 opposes TIGIT to disrupt Tregs in melanoma (20). However, the role of CD226 in modulating the functions of Tregs in EAE remains unclear.
To better elucidate the role of CD226 in CD4+ T subsets, especially in Tregs, we generated CD226 knockout (Cd226−/−) mice and assessed the role of this protein in CD4+ Foxp3− traditional T (Tconv) cells and CD4+ CD25+ Foxp3+ Tregs during EAE pathogenesis. We observed that Tconv cells and Tregs from EAE mouse model spleens showed differential expression of CD226 and that Cd226−/− mice were more resistant to EAE than wild-type (WT) mice. Thus, we speculated that the CD226 deletion inhibits the pathological immune response in the EAE model. After comparing the number of Tregs and Th17 cells in the CNS and spleens of mice, we observed the presence of more Tregs but fewer Th17 cells in the spleens, and Th17 cell infiltration into the CNS was decreased in the absence of CD226 during EAE. To further assess whether CD226 is associated with Treg functions, we sorted Tregs from splenocytes and collected in vitro-derived induced regulatory T cells (iTregs) to assess their proliferation and suppressive capacity. We demonstrated that CD226 deficiency facilitates the Treg cell-mediated suppression of autoimmune responses in EAE mice. Then, we sorted Tregs from splenocytes, generated iTregs in vitro and observed that the Akt and Erk signaling pathways are involved in Cd226−/− Treg proliferation and function. These findings collectively indicate that CD226 is a key molecule in the Treg-mediated suppression of autoimmune responses because it inhibits Treg proliferation. Thus, we provide further mechanisms by which CD226 molecules are involved in Treg functions in EAE and evidence for the potential therapeutic effect of targeting CD226 in autoimmune diseases.
Materials and Methods
Mice
WT C57BL/6 mice were purchased from the Nanjing Biomedical Research Institute of Nanjing University (Nanjing, China). CD226 knockout (Cd226−/−) mice in a C57BL/6 background were a kind gift from Professor Marco Colonna. To generate homozygous Cd226−/− mice, the Cd226−/− mice were back-crossed to C57BL/6 mice (8 weeks) and then propagated by Cd226+/− × Cd226+/− mating. The WT (Cd226+/+) mice used as controls in our experiments were the littermates of the Cd226−/− mice. All the mice were bred under specific pathogen-free (SPF) conditions at the Experimental Animals Center of the Fourth Military Medical University. All experiments were approved by the Scientific Investigation Board of the Fourth Military Medical University, Xi'an (permit number XJYYLL-2014433). All animals were treated according to the Guide for the Care and Use of Laboratory Animals (NIH, Bethesda, USA).
Induction and Assessment of the EAE Model
To induce EAE, mice were subcutaneously immunized in their flanks with 200 μg of MOG35−55 (purity >98%, GT10451-0614, Bankpeptide Biotec, China) in complete Freund's adjuvant (CFA; F-5881, Sigma, St. Louis, MO, USA) containing 4 mg of a thermally inactivated tuberculosis strain (2240273, Difco, Lawrence, USA). On days 0 and 2, the immunized mice were intraperitoneally injected with 200 ng of Bordetella pertussis toxin (P2980, Sigma, St. Louis, MO, USA) (21). The mice were monitored and weighed daily. The clinical score of mouse EAE was determined according to the following judging criteria: 0, no symptom and disease; 1, limp tail; 2, hind-limb weakness; 3, partial hind-limb paralysis; 4, complete paralysis of one or more limbs; and 5, moribund state or dead (21).
Cell Isolation and Culture
Fifteen to eighteen days after immunization, the spleens were removed, and Tregs were isolated using a CD4+CD25+ regulatory T cell isolation kit (130-091-041, MACS Miltenyi Biotec, Germany) following the manufacturer's instructions. To sort purified CD4+ T cells using magnetic beads, erythrocyte-depleted splenocyte suspensions from Cd226−/− or WT mice were negatively selected using the Mojosort™ Mouse CD4 T Cell Isolation kit (480006, Biolegend, San Diego, CA, USA). The purified CD4+ T cells (cell purity >95%) were cultured in RPMI 1640 medium and stimulated with plate-bound anti-CD3 (3 μg/ml, LEAF™ Purified anti-mouse CD3ε, 100313, Biolegend, San Diego, CA, USA) and soluble anti-CD28 (5 μg/ml, LEAF™ Purified anti-mouse CD28, 102111, Biolegend, San Diego, CA, USA) in the presence of recombinant murine IL-2 (2 ng/ml, 212-12, Peprotech, Cranbury, NJ, USA).
To prepare the purified naïve CD4+ T cells, erythrocyte-depleted splenocyte suspensions from Cd226−/− or WT mice were negatively selected using a Mojosort™ Mouse CD4 Naïve T Cell Isolation kit (480039, Biolegend, San Diego, CA, USA). The purity of naïve CD4+ T cells was >95%. A 96-well plate was coated with 3 μg/ml of anti-CD3 antibody (100313, Biolegend, San Diego, CA, USA) in PBS at 4°C overnight. Subsequently, soluble anti-CD28 (5 μg/ml, 102111, Biolegend, San Diego, CA, USA) and recombinant TGF-β1 (5 ng/ml, 100-21, Peprotech, Cranbury, NJ, USA) were added, and the cells were incubated for 3 days to polarize the iTregs (21).
CFSE Labeling and iTreg Inhibition Assay
To determine the iTreg proliferation ability, iTregs were labeled for 8 min at 37°C with 2.5 μM carboxyfluorescein diacetate succinimidyl ester (CFSE) according to the manufacturer's protocol (423801, Biolegend, San Diego, CA, USA). Then, the iTregs were washed three times with RPMI 1640 medium and cultured with plated-bound anti-CD3 (5 μg/ml, 100302, Biolegend, San Diego, CA, USA) and soluble anti-CD28 (5 μg/ml, 102111, Biolegend, San Diego, CA, USA) in RPMI 1640 complete medium with 10% FBS for 3 days. To determine the inhibitory activity of the iTregs, immunogenic bead-sorted CD4+ T cells labeled with CFSE were used as responders. The CD4+ T cells were cultured in 96-well plates with FACS-sorted CD4+CD25+ iTregs for 5 days at various ratios in medium supplemented with soluble anti-CD3 (5 μg/ml) and anti-CD28 (5 μg/ml).
CNS Tissue Isolation and Histology Assay
Mouse lumbar spinal cords and brains tissue were removed at the peak of EAE after cardiac perfusion with PBS and fixed in 4% paraformaldehyde (PFA; P-6148, Sigma, St. Louis, MO, USA). Fixed tissues were washed with ethanol, embedded in paraffin, and used to prepare 20-μm cross-sections that were stained with Luxol fast blue (LFB) to visualize demyelination and H&E to assess cellular infiltration. Spinal cords were used to prepare 20-μm longitudinal sections or cross-sections for immunohistochemical staining for histopathological assessments. All images were captured using an Olympus microscope (Olympus Corporation, Tokyo, Japan), and quantification was performed using ImageJ Pro (Rawak Software Inc., Stuttgart, Germany). For immunofluorescence assays, CNS tissues were fixed in 4% PFA for 10 h, rehydrated in a 30% sucrose solution for 24 h and frozen in OCT for cross-sectioning. Brain tissues were blocked with H2O2 and then stained with anti-Foxp3 (bsm-52079R, Bioss, China) or anti-RORγt (bs-23110R, Bioss, China) antibodies at 4°C overnight. On the second day, The Alexa Fluor 488 conjugated Goat anti-Rabbit (ab150081, abcam, USA) as secondary antibodies were used following the manufacturer's instructions. All images were captured using a Zeiss 710 LSM confocal microscope (Carl Zeiss Inc., Germany). RORγt+ or Foxp3+ cells were quantified as the percentage of the total cells stained with DAPI in each section. All slides were blinded during the assessment, and at least four non-consecutive sections of the lumbar spinal cord or brain of each animal were evaluated by two individuals. The number of animals analyzed and used in the experiment are indicated in the figure legends.
Isolation of Mononuclear Cells in the Spinal Cord and Brain
The spinal cords and brains of mice were removed at the peak of EAE after cardiac perfusion and washed twice with fresh pre-cooled PBS. After homogenization and collection of these tissues, the CNS mononuclear cells were harvested by centrifugation with 70–30% Percoll gradients (28-9038-34, GE Healthcare, Sweden), passed through a 70-μm filter and then washed with RPMI 1640 medium according to the manufacturer's protocol. The viability of the cells was detected using trypan blue staining (22).
Flow Cytometry
The expression of cell surface molecules was detected by staining with antibodies against CD4 (Percp anti-mouse CD4, 100538, Biolegend, San Diego, CA, USA), CD69 (FITC anti-mouse CD69, 104505, Biolegend, San Diego, CA, USA), CD25 (PE anti-mouse CD25, 102007, Biolegend, San Diego, CA, USA), CD226 (APC anti-mouse CD226, 125509, Biolegend, San Diego, CA, USA), and TIGIT (APC anti-mouse TIGIT, 131510, Biolegend, San Diego, CA, USA), diluting each antibody according to the manufacturer's instructions. The in vitro apoptosis of iTregs after polarization from naïve CD4+ T cells was determined using a FITC Annexin V Apoptosis Detection kit with propidium iodide (PI; 640914 Biolegend, San Diego, CA, USA).
To examine the intracellular expression of the cytokines IFN-γ (PE anti-mouse IFN-γ, 505807, Biolegend, San Diego, CA, USA), IL-4 (PE anti-mouse IL-4, 504104, Biolegend, San Diego, CA, USA), IL-10 (PE anti-mouse IL-10, 505008, Biolegend, San Diego, CA, USA), and IL-17A (PE anti-mouse IL-17A, 506904, Biolegend, San Diego, CA, USA), the cells were stimulated with Cell Activation Cocktail (with Brefeldin A) (423303, Biolegend, San Diego, CA, USA) for 6 h according to the manufacturer's protocols. To determine the amount of Foxp3+ and Ki67+ cells in the population, the cells were sequentially fixed, permeabilized (Fixation/permeabilization Diluent, 00-5223, eBioscience, San Diego, CA, USA) and stained with Foxp3 (Alexa Fluor 488 anti-mouse FOXP3, 320011, Biolegend, San Diego, CA, USA) or Ki67 (PE anti-mouse Ki67, 652403, Biolegend, San Diego, CA, USA).
Quantitative Reverse Transcriptase-Polymerase Chain Reaction (RT-qPCR)
RNA was isolated with RNAiso Plus (9109, TaKaRa, Japan) according to the manufacturer's protocol. The cDNA was synthesized with PrimeScript RT Master Mix (RRO36A, TaKaRa, Japan), and PCR was performed using SYBR PremixEx Taq™ II (RR820A, TaKaRa, Japan). The sequences of primers used for Tregs and Th17 cell-related molecules are listed in Supplemental Table 1. The primers were purchased from Applied Biosystems (AUGCT, China). The samples were amplified over 40 cycles using the following thermocycling program: 15 s at 95°C and 1 min at 60°C. GAPDH gene expression was used as an endogenous reference to calculate relative mRNA expression.
Western Blotting
A total of 5 × 106 isolated cells or induced iTregs were stimulated with anti-CD3 (5 μg/ml)/anti-CD28 (5 μg/ml) plus IL-2 (2 ng/ml) in the presence or absence of TGF-β1 (5 ng/ml) for the indicated times. The cells were harvested and then lysed using RIPA (70166, Sigma, St. Louis, MO, USA) to obtain protein. The protein concentration was determined using a Pierce BCA Protein Assay kit (#23225, Thermo, USA), 15 μl of protein lysate was loaded onto 8% SDS-PAGE gels, and the proteins were blotted onto nitrocellulose membranes. The membranes were blocked with 5% skim milk (70166, Sigma-Aldrich, St. Louis, MO, USA) and incubated at 4°C for 12 h, which was followed by an incubation with horseradish peroxidase-conjugated secondary antibodies. The expression of the indicated proteins was detected with antibodies against the following: Akt (#207, Cell Signaling, USA), phospho-Akt (Ser473) (#207, Cell Signaling, USA), p44/42 MAPK (Erk1/2) (137F5) (#5594, Cell Signaling, USA), phospho-p44/42 (Erk1/2) (#5595, Cell Signaling, USA) and β-actin (#4970, Cell Signaling, USA). The antibodies were diluted 1:2,000 (phospho-antibodies and β-actin antibodies) or 1:1,000 (Akt and Erk1/2 antibodies). Mouse anti-rabbit IgG mAb (HRP conjugate) (#93702, Cell Signaling, USA) was used as a secondary antibody at a 1:2,000 dilution. The protein bands were detected using an ECL detection system and visualized with a Tanon™ High-sig ECL Western Blotting Substrate kit according to the manufacturer's instructions (180-500, Tanon, China).
Statistical Analysis
Statistical analysis was performed using GraphPad Prism 6 (Prism Software, Lake Forest, CA). For parametric analysis, Student's t-test was used. Statistical comparison of EAE severity and body weight between experimental groups was performed using a non-parametric Mann-Whitney U-test (two-tailed). The data are presented as the mean ± standard error of the mean (SEM). Differences achieving values of P < 0.05 were considered significant, while P > 0.05 was considered non-significant (ns). FlowJo V10 (Tree Star, CA, USA) was used to analyse flow cytometry data. The histology assays were performed with Image-Pro software.
Results
Tregs Fail to Upregulate CD226 Expression Levels During EAE Conditions
CD226 is crucial for the activation of CD4+ T cells (23), which contributes to the LFA-1 costimulatory signaling that promotes Th1 cell differentiation (3). To determine whether CD226 is involved in the function of CD4+ T cell subsets, we first evaluated the level of CD226 expression of total spleen CD4+ T cells, CD4+ Foxp3− Tconv cells and CD4+CD25+Foxp3+ Tregs of WT mice. Under healthy conditions, the expression levels of CD226 in total CD4+ T cells and their subset cells were comparable. Notably, the level of CD226 expression was upregulated in total CD4+ T cells and in Tconv cells under EAE conditions compared with that observed under healthy conditions, in agreement with previous reports that CD226 plays an important role in promoting CD4+ T cell activation in response to autoimmune diseases (24, 25). However, mouse spleen Tregs failed to upregulate CD226 under EAE conditions compared with that observed under healthy conditions (Figure 1A). These observations suggest a potential differential role of CD226 in regulating the function of CD4+ T cell subsets during healthy and EAE conditions. Because TIGIT and CD226 both bind the ligands CD155 and CD112, we next asked whether TIGIT is also differentially expressed in CD4+ T subsets in mice during EAE conditions. The results revealed that CD4+ T subsets expressed higher levels of TIGIT during EAE pathogenesis than that observed during healthy conditions. Notably, no differential TIGIT expression was observed among CD4+ T cell subsets under healthy or EAE conditions (Figure 1B). Fourcade et al. reported a low CD226/TIGIT ratio in Tregs that was correlated with enhanced Treg stability and function in melanoma (20). Therefore, we speculate that the differential expression of CD226 in CD4+ T subsets during EAE can affect the function of Tregs.
Figure 1. Tregs fail to upregulate CD226 at the peak of EAE. (A) The percentage of CD226+ cells of the total CD4+ T cells, CD4+CD25+ Foxp3+ Tregs or CD4+Foxp3− CD4+ Tconv cells derived from the spleens of WT and WT EAE mice at the peak of EAE (days 15–18 after MOG35−55 immunization) was assessed by flow cytometry (FCM) (n = 10). (B) The percentage of TIGIT+ cells pf the total CD4+ T cells, CD4+CD25+Foxp3+ Tregs or CD4+Foxp3− T cells derived from the spleens of WT and WT EAE mice (at the peak of EAE) were assessed by FCM (n = 10). The results represent five independent experiments (A,B). The data are presented as the mean ± SEM. Frequencies are displayed below the histograms. nsP > 0.05, *P < 0.05, **P < 0.01.
Cd226–/– Mice Are Less Susceptible to EAE and Lower Levels of Infiltrated Th17 Cells in the CNS of Cd226–/– Mice
To evaluate the function of CD226 in CD4+ T subset cells, we constructed Cd226−/− mice with knocked out CD226 (Supplemental Figure 1). We investigated the difference between Cd226−/− and WT mice under inflammatory conditions and used the MOG35−55-induced EAE model to monitor the pathological effect of CD226. We noticed that EAE could be induced in both Cd226−/− and WT mice with 100% incidence, and no mice died in either group during EAE. We then tested the outcome of these two groups during the development of EAE. Our results showed that WT mice progressively developed EAE based on clinical scoring (Figure 2A), with a maximum mean score of 4.1 ± 0.23, while Cd226−/− mice showed a delayed onset of EAE (maximum mean score of 3.1 ± 0.1). We also observed that CD226 knockout mice showed suppressed disease progression and attenuated clinical scores induced by MOG35−55 (Figure 2A). Moreover, Cd226−/− mice tended to show reduced weight loss (days 4–6 and 20–28 after MOG35−55 immunization), a feature associated with EAE progression (26), although this effect was not significant (Supplemental Figure 2A). These data collectively indicated that CD226 deficiency in EAE mice may alleviate the severity of inflammation, which is consistent with previous studies showing that mice treated with an anti-CD226 polyclonal antibody (pAb) in vivo were resistant to EAE development and progression (27).
Figure 2. Cd226−/− mice are less susceptible to EAE, and lower levels of Th17 cells were infiltrated into the CNS of Cd226−/− mice during EAE. (A) Cd226−/− and WT mice were immunized to induce EAE. The clinical score was monitored at the indicated days after immunization with MOG35−55 in CFA (n = 16). EAE scores were analyzed by a non-parametric Mann-Whiney U-test (two-tailed). The results represent eight independent experiments. (B) Mice were killed at the peak of EAE. Total mononuclear cells infiltrated in the CNS of WT and Cd226−/− mice were calculated (n = 6). (C) LFB staining of the lumbar region of the spinal cord (cross-sections) from WT and Cd226−/− mice at the peak of EAE (n = 6). Demyelination of representative spinal cord sections is indicated by loss of blue staining (scale bars indicate 200 and 50 μm for lower and higher magnification, respectively), and the total demyelinated area was measured with ImageJ. (D) Histological analysis of lymphocyte infiltration in the lumbar region of the spinal cord (cross-sections) of the indicated mice by H&E staining (scale bars indicate 200 and 50 μm for lower and higher magnification, respectively) (n = 6). (E) IL-17A expression in the lumbar region of the spinal cord (cross-sections) at days 15–18 post-immunization was detected by immunohistochemical staining (scale bars indicate 200 and 50 μm for lower and higher magnification, respectively) (n = 6). RORγt (F) and Foxp3 (G) expression in the brains of Cd226−/− mice and WT littermates at the peak of EAE were detected by immunofluorescence staining using RORγt (green) or Foxp3 (green) antibodies, respectively. Nuclei are shown in blue (DAPI) (3 cross-sections of brain per mouse, n = 6). The white arrowhead indicates Th17 cells or Tregs. Scale bar, 100 μm. The results represent three independent experiments (B–G). The data are presented as the mean ± SEM. nsP > 0.05, *P < 0.05, **P < 0.005.
Next, we observed fewer mononuclear cell infiltrates in the spinal cords and brains of Cd226−/− mice than in WT mice at the peak of EAE (Figure 2B). LFB staining results revealed that demyelination in the lumbar region of the spinal cord was lower in Cd226−/− mice than that observed in WT mice (Figure 2C), and the haematoxylin-eosin (H&E) staining results showed a reduction in lymphocyte infiltration in the lumbar region of the spinal cord of Cd226−/− mice during the peak of EAE (Figure 2D). EAE is a myelin-specific autoreactive Th17 and Th1 cell-mediated inflammatory disease (28), and Th17 cells have been reported to have a greater pathogenic impact on the development of EAE than Th1 cells (29). Immunohistochemical analysis showed that infiltration of IFN-γ+ cells in the brains of Cd226−/− mice was comparable to that observed in WT mice at the peak of EAE (Supplemental Figure 2B). We then examined IL-17A expression by immunohistochemical staining and detected fewer IL-17A+ cells in the lumbar spinal cord (cross-sections) of Cd226−/− EAE mice compared to that observed in WT EAE mice (Figure 2E). Because the longitudinal sections clearly highlight the increased extravasation from the spinal cord fluid compared with that observed in the transversal sections at the level of the ependymal channel, we also used the transversal sections of lumbar spinal cords to identify inflammatory infiltrates. Notably, we also observed decreased IL-17A+ cell infiltration in the lumbar spinal cords of Cd226−/− mice during EAE (Supplemental Figure 3A), indicating that CD226-deficient mice during EAE had reduced immune activation compared with WT mice during EAE. From these results, we presumed that the CD226 deficiency in mice led to decreased EAE susceptibility, in part because of decreased inflammatory Th17 cell infiltration into the CNS. Because the results of our previous study showed that CD226 is robustly expressed in the brain (30), we next investigated whether deletion of CD226 in mice reduces the number of cells infiltrating the brain and damage. We observed that both infiltrating cells and demyelination were reduced in the brain tissue of Cd226−/− compared with that observed in WT mice (Supplemental Figures 3B,C). RORγt is a transcription factor that is unique to Th17 cells and directs the polarization of naïve CD4+ T cells to Th17 cells (31). The transcription factor Foxp3 is a key factor in the regulation of Treg-mediated immunosuppressive responses (32). Immunofluorescence staining results showed that the amount of RORγt protein was reduced (Figure 2F) and that Foxp3 protein was increased in the brains of Cd226−/− mice compared with that observed in their WT counterparts during the peak inflammation period of EAE (Figure 2G). These data collectively suggest that the deletion of CD226 may lead to a reduced inflammatory response in mice that is associated with high numbers of Tregs and reduced infiltration of Th17 cells in the CNS.
Decreased Numbers of Th17 Cells and Increased Numbers of Tregs in the Spleens of Cd226–/– EAE Mice
IFN-γ is a pro-inflammatory cytokine that can enhance the degree of inflammation in EAE (33). To investigate whether CD226 deficiency could inhibit IFN-γ production, the plasma level of IFN-γ in Cd226−/− mice was examined in the EAE model. The level of IFN-γ in Cd226−/− mice was apparently lower than that observed in WT mice during EAE pathogenesis (Figure 3A). Moreover, mice deficient in CD226 showed increased levels of the inhibitory cytokine IL-10 in plasma (Figure 3A). To investigate whether CD226-deficient mice were prone toward a loss of homeostasis of CD4+ T cell subsets in the periphery, we compared representative cytokines produced by CD4+ T cell subsets between Cd226−/− and WT mice under healthy conditions (Figure 3B). IFN-γ and IL-17A are the primary effector cytokines of Th1 and Th17 subsets, respectively. The results showed that the IFN-γ+ CD4+ T cell compartment was slightly decreased, while that of the IL-17A+ CD4+ T cell subset was normal in Cd226−/− mice. In contrast, the levels of IL-10 and IL-4, the signature chemokines for Tregs and Th2 cells, respectively, were clearly increased in the CD4+ T cells of Cd226−/− mice (Figure 3B). These results collectively indicated an intrinsic role of CD226 in regulating cytokine production in CD4+ T cell subsets.
Figure 3. Lower levels of Th17 cells and higher levels of Tregs were observed in the spleen of Cd226−/− EAE mice. (A) The plasma levels of IFN-γ and IL-10 in Cd226−/− and WT mice during EAE pathogenesis were assessed by ELISA (n = 8). (B) Protein expression of IFN-γ, IL-4, IL-17A and IL-10 in sorted CD4+ T cells from splenocytes in Cd226−/− mice and WT littermates was assessed by intracellular staining. The numbers in each quadrant show the percentage of the relevant cell population (n = 8). (C) Splenocytes were stimulated in vitro with PMA (phorbol myristate acetate), ionomycin and brefeldin A in 10% FBS/RPMI 1,640 for 6 h. FCM data analysis of CD4+ T cell subsets for cytokines released from the spleens of Cd226−/− or WT mice was conducted on days 15–18 after immunization with MOG35−55 (gated on total CD4+ T cells, with frequencies on the left). The proportions of Th1, Th2, Th17 cells and Tregs were determined by intracellular cytokine staining (n = 6). (D) The relative mRNA levels of IFN-γ, IL-4, IL-17A, and IL-10 in CD4+ T cells isolated from the spleens of Cd226−/− or WT mice at days 15–18 after immunization with MOG35−55 were determined by RT-qPCR (n = 6). (E) The relative mRNA levels of Foxp3 and RORγt in CD4+ T cells isolated from the splenocytes of WT or Cd226−/− mice on days 15–18 after immunization with MOG35−55 were determined by RT-qPCR (n = 6). The results represent at least three independent experiments (A–E). The data are presented as the mean ± SEM. nsP > 0.05, *P < 0.05, **P < 0.005, ***P < 0.001.
The reduction of EAE severity in Cd226−/− mice prompted us to examine whether CD226 is involved in regulating commitment to the CD4+ T cell lineage. Therefore, we investigated how these CD4+ T sub-populations were affected by CD226 deletion under EAE conditions. At days 15–18 after MOG35−55 immunization, the expression levels of IFN-γ, IL-4, IL-17, and IL-10 in CD4+ T cells sorted from the splenocytes of Cd226−/− or WT mice were evaluated by flow cytometry (Figure 3C). During the peak stage of EAE progression, although the production of IFN-γ in CD4+ T cells was greatly enhanced in both Cd226−/− and WT mice compared with that observed in healthy mice, we did not observe a significant difference in the level of this cytokine between Cd226−/− and WT mice. We further evaluated whether CD226 deficiency could affect cytokine production by Th2 cells and observed that CD4+ T cells from Cd226−/− mice had an IL-4 response to MOG35−55 that was comparable to that of the WT littermate controls. Th17 cells have been reported to be major factors involved in the development and progression of EAE (34). Notably, we observed that number of CD4+ IL-17A+ T cells was not increased in Cd226−/− mice but was sharply increased in WT mice. The increased production of IFN-γ and IL-17A in the WT mice during EAE largely accounted for the exacerbated Th1 cells and Th17 autoimmune response cells, highlighting the crucial role of CD226 in CD4+ T cell participation in Th1 and Th17 reactions. In contrast to the role of Th17 cell-related IL-17A in exacerbating EAE pathogenesis, IL-10 is a defining anti-inflammatory cytokine for Tregs, playing an essential role in negatively regulating autoimmune responses (33). Our results showed an increase in IL-10 production from CD4+ T cells of Cd226−/− mice compared with that observed in WT mice during EAE. Thus, we speculated that the Tregs of Cd226−/− mice are activated under EAE conditions (Figure 3C). Taken together, the alleviation of EAE by the deletion of CD226 in mice likely occurred by restoring the balance of Tregs/Th17 cells. To further verify these results at the mRNA level, we sorted CD4+ T cells from the spleens of Cd226−/− and WT mice at the peak of EAE and detected the mRNA expression levels of the cytokines IFN-γ, IL-4, IL-17A, and IL-10 and the transcription factors RORγt and Foxp3 by RT-qPCR. Consistent with the flow cytometry (FCM) results, we observed a decrease in IL-17 but a marked increase in IL-10 levels, with no significant changes observed in IFN-γ and IL-4 in Cd226−/− EAE mice (Figure 3D). We also observed that the level of Foxp3 mRNA was clearly increased and that of RORγt mRNA was decreased in splenic CD4+ T cells from Cd226−/− EAE mice (Figure 3E). From these results, we concluded that deletion of CD226 decreased the level of Th17 cells but facilitated Tregs in the spleens of Cd226−/− mice during EAE.
Cd226–/– Tregs Are Highly Proliferative and Suppressive in vivo
At the peak of EAE, we observed that the percentage of Tregs in splenic CD4+ T cells was increased upon CD226 deletion (Figure 4A). To elucidate the mechanism responsible for the higher percentage of Tregs in CD4+ T cells from Cd226−/− EAE mice, we further examined Treg proliferation and suppression in vivo. Freshly isolated Tregs from Cd226−/− healthy mice expressed slightly higher percentages of the proliferation marker Ki67 than WT mice. At 15–18 days after immunization with MOG35−55, the expression of Ki67 in the freshly isolated Tregs from WT mice was clearly decreased, while that of the Tregs from Cd226−/− mice was not. Notably, under EAE conditions, the expression of Ki67 in Cd226−/− Tregs was higher than that observed in WT Tregs, indicating an elevated level of Cd226−/− Treg proliferation (Figure 4B). We next wanted to determine whether the deletion of CD226 affected the proliferation of Tregs after TCR stimulation. To this end, we assessed Ki67 expression in Tregs with anti-CD3/anti-CD28 antibodies after 3 h of culturing. Compared with their WT EAE counterparts, the Tregs from Cd226−/− EAE mice showed higher expression of Ki67 (Figure 4B). In contrast, freshly isolated Tconv cells from Cd226−/− EAE mice expressed lower levels of Ki67 than their WT counterparts during EAE pathogenesis. This pattern was particularly notable after anti-CD3/anti-CD28 stimulation for 3 h. These results demonstrated that CD226 depletion led to high proliferation of Tregs under EAE conditions, whereas Tconv cells were less activated than the WT mice (Figure 4C).
Figure 4. Cd226−/− Tregs are highly proliferative and suppressive in vivo. (A) The percentages of Tregs in spleen CD4+ T cells from CD226−/− and WT littermate mice on days 15–18 after treatment with MOG35−55 (n = 6). (B) Percentage of Ki67+ cells in CD4+Foxp3+ Tregs freshly isolated or after 3 h of culturing with anti-CD3 (5 μg/ml)/anti-CD28 (5 μg/ml) from spleen cells of Cd226−/− and WT mice on days 15–18 after MOG35−55 immunization by FCM (n = 3). (C) Percentage of Ki67+ cells in CD4+Foxp3− Tconv cells freshly isolated or after 3 h of culturing with anti-CD3 (5 μg/ml)/anti-CD28 (5 μg/ml) from splenocytes of Cd226−/− and WT mice at the peak of EAE were detected by FCM (n = 3). Expression of CD69 (D) or IL-10 (E) in splenic CD4+ CD25+ Foxp3+ Tregs from Cd226−/− and WT mice under healthy conditions or EAE pathogenesis were detected by FCM (n = 6). The data are presented as the mean ± SEM. nsP> 0.05, *P < 0.05, **P < 0.005, ***P < 0.001.
To further confirm these results, we examined the activation status of Tregs from Cd226−/− mice during EAE. The level of CD4+Foxp3+ Tregs from Cd226−/− mice with an acute activated CD69 phenotype was increased compared with that observed in WT mice, especially during EAE pathogenesis (Figure 4D). Based on these results, we explored whether this enhanced proliferation in Tregs was associated with dysregulated cytokine production. IL-10 has been demonstrated to play an important role in the suppression of Th17 cell-mediated inflammation (35). Therefore, we analyzed the production of IL-10 from Tregs in Cd226−/− mice under healthy conditions and during EAE inflammatory conditions. The results showed that Tregs in Cd226−/− mice generated large amounts of IL-10, and this expression was notably increased during EAE inflammation (Figure 4E). TGF-β plays a pivotal role in regulation of the differentiation and function of Tregs (36). So we next magnetically sorted Tregs (cell purity ≥94%) (Supplemental Figure 4A) from the spleens of Cd226−/− and WT mice at the peak of EAE and detected the mRNA expression level of TGF-β. The results showed that TGF-β mRNA was largely normal in Cd226−/− EAE mice compared with WT EAE mice, suggesting that the TGF-β may not involve in the enhanced function of Tregs (Supplemental Figure 4B). Taken together, these results indicated that the deletion of CD226 led to enhanced Treg proliferation and increased IL-10 production.
Cd226−/− iTregs Are Highly Proliferative and Suppressive in vitro
Although the deletion of CD226 facilitated Treg proliferation and IL-10 production during inflammatory conditions in vivo, the relationship between CD226 deletion and Treg in vitro function remains unclear. To investigate whether the deletion of CD226 could also influence the suppressive function of Tregs in vitro during EAE, we decided to preliminarily investigate the abilities of iTreg cells. We isolated naïve CD4+ T cells (CD4+CD62L+) from WT EAE and Cd226−/− EAE mice and cultured them for 3 days under Treg-polarizing conditions. The iTreg proliferation was assessed by FCM after incubating overnight with plate-bound anti-CD3 at 4°C and soluble anti-CD28 stimulation for 3 days in vitro. Our results showed that CD226-deficient naïve CD4+ T cells had an enhanced ability to induce iTregs comparable to that of WT mice (Figure 5A). Moreover, the rate of CFSE-labeled iTreg proliferation was higher than that observed in WT mice (Figure 5B), indicating that the iTregs induced from Cd226−/− EAE mice remained energetic in vitro, to an even higher extent than those from WT EAE mice. To determine whether the loss of CD226 in iTregs is linked to apoptosis, we stained iTregs with PI and annexin V and observed a comparable percentage of apoptotic cells between WT and Cd226−/− iTregs, indicating that CD226-deficient iTregs did not display decreased apoptosis relative to their CD226-sufficient counterparts (Supplemental Figure 4C). Next, to directly evaluate whether the immunosuppressive activity of CD226-deficient iTreg cells was affected in vitro, we used an in vitro suppression assay. Responder CD4+ T cells were magnetically sorted from healthy WT mice and labeled with CFSE. The iTregs induced from naïve CD4+ T cells of Cd226−/− EAE or WT EAE mice were then cultured with varying amounts (as indicated) of labeled responder CD4+ T cells in the presence of anti-CD3/CD28 for 5 days, after which the responder cell proliferation was determined. The results confirmed that CD226-deficient iTregs highly suppressed responder cell function in vitro and showed an enhanced ability to suppress responder cell proliferation under TCR-stimulated conditions compared with the iTregs induced in WT EAE mice (Figure 5C). These results further demonstrated that the deletion of CD226 facilitated the suppressive capacity of Tregs.
Figure 5. Cd226−/− iTregs are highly proliferative and suppressive in vitro. (A) Naïve CD4+ T cells from WT and Cd226−/− mouse spleens from days 15–18 after MOG35−55 immunization were magnetically sorted. Then, the cells were cultured under iTreg polarizing conditions [plate-coated anti-CD3 (3 μg/ml), soluble anti-CD28 (5 μg/ml), IL-2 (2 ng/ml)] and recombinant TGF-β (5 ng/ml), and Foxp3 expression was measured by FCM after 3 days of culture (n = 6). (B) The proliferation of iTregs was assessed by FCM. iTregs were labeled with CFSE and cultured in the presence of anti-CD3 (5 μg/ml) and anti-CD28 (5 μg/ml) for 3 days, and the proliferative capacity was detected 3 days later (n = 6). (C) The suppressive capacity of iTregs was detected by FCM. CD4+CD25+ iTregs induced from naïve CD4+ T cells of WT or Cd226−/− mice were sorted and co-cultured with the indicated ratios of CFSE-labeled responder CD4+ T cells from WT mice for 5 days in the presence of anti-CD3 (5 μg/ml) and anti-CD28 (5 μg/ml) (n = 3). The results represent three independent experiments (A–C). The data are presented as the mean ± SEM. nsP > 0.05, *P < 0.05.
Akt and Erk Signaling Pathways Are Involved in Cd226–/– Treg Proliferation and Function
Previous studies have shown that Akt and Erk signaling pathways are involved in regulating T cell survival, proliferation, and differentiation (37, 38). To address whether the loss of CD226 can affect the Akt and Erk signaling pathways, which are associated with Treg proliferation and suppression, we observed the biochemical mechanisms of CD226 in vivo in sorted Tregs and in vitro-generated iTregs by assessing Akt and Erk signaling. After stimulating freshly isolated Tregs with anti-CD3/CD28 in the presence of IL-2 for 2 h, we observed that Cd226−/− Tregs showed higher levels of phosphorylated-Akt (ser473) and phosphorylated p44/42 (Erk1/2) than WT Tregs (Figure 6A). In contrast, the Cd226−/− Tconv cells showed decreased activation of Akt signaling and reduced activation of Erk signaling compared with that observed for WT Tconv cells (Figure 6B). Next, we evaluated whether the enhanced proliferation of Cd226−/− iTregs in vitro was associated with activation of the Akt and Erk signaling pathways by assessing the phosphorylation levels of Akt (ser473) and p44/42 (Erk1/2) in iTregs differentiated from naïve WT and Cd226−/− CD4+ T cells for 96 h. As expected, the Cd226−/− iTregs exhibited higher levels of phosphorylation of both Akt and Erk than WT iTregs (Figure 6C). These results confirmed that the enhanced proliferation of Cd226−/− Tregs may be associated with activated Akt and Erk signaling.
Figure 6. Higher levels of Akt and Erk signaling occur in Cd226−/− Tregs. Splenic Tregs (A) and Tconv cells (B) magnetically isolated from WT or Cd226−/− mice were stimulated with anti-CD3 (5 μg/ml), anti-CD28 (5 μg/ml) and IL-2 (2 ng/ml) for 2 h, after which p44/42 (Erk1/2), phospho-p44/42 MAPK (Erk1/2), Akt and phosphorylated-Akt (Ser473) were detected by Western blotting (n = 6). (C) Naïve CD4+ T cells magnetically sorted from WT and Cd226−/− mouse spleen were cultured under iTreg cell polarizing conditions for 96 h [plate-bound anti-CD3 (3 μg/ml) plus soluble anti-CD28 (5 μg/ml), IL-2 (2 ng/ml) and recombinant TGF-β (5 ng/ml)]. The levels of Erk1/2, phosphorylated-Erk (p-Erk1/2), Akt and phosphorylated-Akt (p-Akt) (Ser473) in iTregs was detected by Western blotting (n = 6). The Western blot results were quantified by ImageJ analysis and are shown as the p-Erk/Erk or p-Akt/Akt ratios. The results represent three independent experiments (A–C). The data are presented as the mean ± SEM. *P < 0.05, **P < 0.005.
Discussion
Several lines of evidence have demonstrated that CD226 plays a crucial role in the formation of immune synapses, and it is primarily considered to be an active receptor of NK and T cells (3, 39). The results of our previous studies demonstrated that mice treated with an anti-CD226 pAb in vivo have markedly decreased EAE susceptibility (27), in agreement with recent data showing that CD226 is involved in the pathogenesis of autoimmune diseases (8, 9). EAE is caused by the breakdown of self-tolerance and eventually leads to myelin-reactive CD4+ T cell infiltration of the CNS to mediate neuronal inflammation (11, 29). Thus, we focused on the function of CD226 in CD4+ T subset cells during EAE. Prior studies showed that the murine CD226/Ig fusion protein can inhibit the production of thymocytes and speculated that CD226 may be involved in the early stage of T cell development (40). Studies in rodents have shown that knockdown of CD226 in naïve CD4+ T cells results in decreased T-bet expression and increased GATA3 expression, as well as demonstrating that CD226 blockade with a neutralizing Ab in vitro can efficiently downregulate IL-17 secretion (41). Because CD4+ T cells play a central role in autoimmunity, and CD226 promotes self-reactive CD4+ T cell activation in the autoimmune response (8, 42), we considered whether CD226 functions by altering the balance of CD4+ T cell subsets involved in the pathogenesis of EAE. Therefore, we developed an EAE mouse model to better understand the unique functions and mechanisms of CD226 in CD4+ T cell lineages under pathological conditions. Tregs are known to suppress the response of myelin-reactive CD4+ Teff and are pivotal in regulating CNS inflammation during EAE (43). Several studies have reported disruptions in the numbers or function of Tregs involved in the pathogenesis of EAE (16), but the factors affecting the stability and function of Tregs are poorly understood. In our study, we observed an increased level of CD226 expression in spleen CD4+ T cells and CD4+ Foxp3− Tconv cells; however, CD226 expression was not upregulated in Tregs under EAE conditions. These observations suggest a potentially distinct role for CD226 in controlling CD4+ T cell lineages, especially in Tregs. Despite evidence of the genetic associations of CD226 with autoimmune diseases and dysfunctional Tregs (7, 44, 45), as well as studies noting that CD226+TIGIT− Tregs are associated with reduced suppressive capacity (46), the exact molecular mechanism and function role of CD226 in Tregs is poorly understood.
To examine whether CD226 mediates the auto-reactive CD4+ T cell response and the immunosuppressive function of Tregs during EAE, we compared the disease development, demyelinating conditions, inflammatory process and distribution of CD4+ T subsets in CNS tissue in Cd226−/− EAE and WT EAE mice. We observed that CD226 deletion delayed the onset and alleviated the development of EAE. Cd226−/− mice tended to show reduced body weight loss at days 4–6 and 20–28 after MOG35−55 immunization, but unfortunately, we did not observe significant differences between the two groups during EAE. We speculate that this result may have been due to the short peak period of EAE and the gradual dampening of disease development after the acute phase. Additionally, the infiltration of inflammatory cells into the CNS was decreased. We also observed a decreased number of RORγt+ cells and an increasing number of Foxp3+ cells that infiltrated into the CNS tissue in Cd226−/− EAE mice. These results collectively suggest that the deletion of CD226 may lead to a reduced inflammatory response in mice, which is most likely associated with maintaining the Treg/Th17 immune balance in the CNS. Recently, the imbalance between Th17 cells and Tregs has been considered to be an important paradigm in the development and pathogenesis of EAE (47). Several studies have demonstrated that the migration of Th17 cells into the CNS is the key pathogenic process in EAE mice (34, 48) and that Foxp3 deficiency is closely associated with spontaneous autoimmunity development (13, 49, 50). CD226 is a co-stimulatory molecule that plays an important role in the activation, expansion and function of Th1 cells (51). Moreover, CD226/CD155 interaction has been demonstrated to regulate the pro-inflammatory (Th1 and Th17) and anti-inflammatory (Th2) balance (41). Based on these findings and our results, we speculated that CD226 is a crucial molecule that regulates auto-reactive Th17 cells and Treg immune responses in EAE. However, additional studies are needed to elucidate the effects of CD226 blockade Ab treatment on the CNS tissue inflammatory responses during EAE pathogenesis.
Based on their distinct cytokine profiles, CD4+ T subsets have different functional properties (52). IL-17 secreted by Th17 cells has been shown to have a pathogenic role in promoting and enhancing autoimmune tissue injuries (53). IL-10, an important mediator with anti-inflammatory properties, is primarily produced by Tregs and can inhibit Th17 cell differentiation in the CD4+ T cell population. We next assessed the frequency and numbers of the CD4+ T subsets of spleen cells at the peak of EAE to understand whether similar changes occur in the peripheral immune organs. In our study, we observed that deletion of CD226 increased the expression of IL-10 and decreased that of IL-17A, whereas it did not notably alter IFN-γ and IL-4 expression in CD4+ T cells during EAE. The administration of IL-10 has been demonstrated to suppress EAE progression (54), and the induction of EAE in IL-17−/− mice was shown to reduce disease severity and promote early recovery (55). Based on our results, we speculate that deletion of CD226 does not greatly affect the Th1 and Th2 cellular immune response but rather alters the balance of Treg/Th17 cells in the EAE model. These results are consistent with a report showing that CD226 costimulatory signaling is associated with LFA-1 to amplify TCR signaling through VAV1, further promoting IL-17 production by CD4+ T cells (56). Additionally, our observation further confirmed that CD226 may play an important role in the activation and effector functions of Th17 cells under EAE inflammatory conditions.
The stable expression of Foxp3 and potent suppressive capacity are two basic characteristics that are maintained in the Treg lineage (57). Another major finding of our study is that deletion of CD226 led to the upregulation of Treg proliferation and enhanced the suppressive function of Tregs during EAE. Recently, studies have demonstrated that CD226 is involved in the function and stability of Tregs (20) and that CD226+TIGIT− Tregs exhibit enhanced methylation in the Treg-specific demethylated region (TSDR) (46), indicating that CD226 may regulate Treg function. In our study, the Tregs in Cd226−/−EAE mice expressed high levels of the proliferation marker Ki67 and the acute activation marker CD69. Tregs are typically stable and able to retain lineage characteristics in vivo. However, during inflammation or other pathological conditions, Tregs may lose Foxp3 expression and then exhibit a reduced suppressive capacity (58). Our results showed that the CD226 deficiency maintained iTreg functions during EAE pathogenesis. We observed that the proliferation of responder CD4+ T cells was decreased after co-culturing with iTregs, indicating that CD226 deletion promoted the suppressor capacity of iTreg cells in vitro. Many studies have demonstrated that decreased IL-10 production by Tregs is linked to MS (16). Treg-secreted IL-10 plays an essential role in the negative regulation of autoimmune responses. Notably, we observed that a significant increase in the expression of IL-10 in CD226-deficient Tregs at the peak of EAE, indicating that the deletion of CD226 maintained the suppressive capacity of Tregs, partially through the promotion of IL-10 signaling.
The Akt and Erk signaling pathways function downstream of TCR and CD28 signaling and are important in the regulation of survival, growth, proliferation and differentiation processes in T cells under varying levels of TCR signaling stimulation (59, 60). Studies have reported a key role for the Akt pathway in the TCR-independent phase of thymic Treg generation (61) and BMP-2, 4, members of the TGF-β superfamily, promote Treg development through the Erk pathway (62). Moreover, Previous studies demonstrated that CD226 triggers signals involving activation of Akt and Erk (63), and the engagement of human CD226 by anti-CD226 antibodies failed to trigger activation of Akt and Erk (64). To determine whether the increased proliferation of Cd226−/− and Cd226−/− iTregs was associated with these pathways, we measured the expression of the Akt and Erk kinases in vitro. Our results demonstrated that Cd226−/− and Cd226−/− iTregs stimulated with anti-CD3/CD28 plus IL-2 exhibited Akt and Erk pathway activation, but Cd226−/− Tconv cells did not. The mechanistic target of rapamycin (mTOR) is a nutrient sensing kinase that functions downstream of Akt (65). mTOR is now well recognized as an important regulator of CD4+ T subsets (66) that influences the development of autoimmune diseases such as MS and EAE (67, 68). mTOR has two distinct signaling complexes, mTOR1 and mTOR2, which have pivotal roles in regulating the differentiation of CD4+ T subsets (69). Our results revealed a high proportion of inflammatory cell infiltration into the CNS in WT but not Cd226−/− mice at the peak of EAE, and Cd226−/− Tconv cells showed decreased activation of Akt signaling. Based on these results, we speculated that the deletion of CD226 in mice blocks the Akt pathway in Tconv cells, which especially influences mTOR1 activation. Rapamycin specifically blocks mTOR1 activation and effectively inhibits T cell proliferation (70), and evidence from mouse studies and clinical trials has demonstrated that blockade of mTOR1 with rapamycin ameliorates the development of EAE and exerts beneficial effects in relapsing/remitting MS (67, 68). These observations correlate with our findings indicating that the deletion of CD226 blocks mTOR1 activation to prevent the differentiation of Th1 and Th17 cells. Keever Taylor and colleagues reported that rapamycin-treated Treg cultures from MS patients had enhanced suppressor functions and contained high levels of CD4+Foxp3+ cells compared with healthy controls, suggesting that blockade of mTOR1 promotes Treg development and function (71). In our studies, we observed the Cd226−/− Tregs had increased Akt activation. Considering the distinct STAT activation functions of mTOR1 and mTOR2 (69, 72), it is possible that mTOR2 or another pathway may be involved in boosting the proliferation and function of Cd226−/− Tregs. Thus, our results indicate that CD226 deletion facilitates the proliferation of Tregs and downregulates the activation of self-reactive CD4+ T cells, partially through activation of the Akt and Erk kinases. These findings are partly consistent with a report showing that blockade of the Erk pathway markedly attenuates Foxp3 expression in TGF-β-primed CD4+ T cells (37).
Taken together, the results of our study have revealed that CD226 acts as an essential molecule that influences the CD4+ T subset-mediated immune response, particularly the autoimmune reactions of differentially regulated Tconv and Tregs. Deletion of CD226 could enforce Treg differentiation and proliferation as well as Treg-mediated repression of Th17 responses. Multiple mechanisms are involved in the maintenance of the suppressive functions of Tregs in Cd226−/− mice during EAE, such as the sustained expression of Foxp3, the production of high levels of the anti-inflammatory cytokine IL-10 and the activation of the Akt and Erk kinases. Nevertheless, an understanding of the CD226-mediated regulation of Treg immune functions is far from complete. Our future studies will utilize a CD226 blocking antibody and conditional CD226 knockout mice to explore the crosstalk between CD226 and intracellular molecule signaling in Tregs. This information will provide support for the therapeutic applications of CD226 blockade in inflammatory diseases.
Data Availability Statement
All datasets generated for this study are included in the article/Supplementary Material.
Ethics Statement
The animal study was reviewed and approved by the Scientific Investigation Board of the Fourth Military Medical University, Xi'an (permit number XJYYLL-2014433).
Author Contributions
LC and BJ designed experiments. NW, SL, JJ, and JX carried out experiments. ZL and HZ analyzed experimental results. LF and HY analyzed FCM data. QM and FJ assisted with NW wrote the manuscript. JL and YS completed the immunohistochemical staining of the revised version. All authors contributed to the article and approved the submitted version.
Funding
This research was supported by the National Natural Science Foundation of China (81571531 and 81872315).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We thank Professor Marco Colonna for the kind gift of the Cd226−/− mice. We thank the 17th International Congress of Immunology for providing us with opportunities to learn and communicate (73).
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2020.01883/full#supplementary-material
Supplemental Figure 1. Efficient CD226 deletion in Cd226−/− mice. Total CD4+ T cells, Tregs (CD4+ CD25+ Foxp3+) and Tconv cells (CD4+ Foxp3−) were gated from the splenocytes of Cd226−/− mice, and the expression levels of CD226 were detected by FCM (n = 8). The data are representative of four independent experiments. The numbers in each quadrant show the percentage of the relevant cell population.
Supplemental Figure 2. Characterization of WT EAE and Cd226−/− EAE mice. (A) The body weight of Cd226−/− and WT mice was monitored daily after immunization with MOG35−55 (n = 16). The results represent eight independent experiments. (B) IFN-γ expression in the brain on days 15–18 post-immunization was detected by immunohistochemical staining (n = 6), and the integrated optical density of IFN-γ was measured with ImageJ. The results represent three independent experiments. nsP > 0.05.
Supplemental Figure 3. Lower levels of infiltrated cells and demyelination in the CNS of Cd226−/− Mice. (A) IL-17A expression in the lumbar region of the spinal cord (longitudinal sections) at days 15–18 post-immunization was detected by immunohistochemical staining (n = 6) (scale bars indicate 100 and 50 μm for lower and higher magnification, respectively). (B) Histological analysis of lymphocyte infiltration in the brain tissue (cross-sections) of the indicated mice by H&E staining (scale bars indicate 50 μm for lower magnification, and 50 μm for higher magnification) (n = 6). (C) LFB staining of the brains (cross-sections) of WT and Cd226−/− mice at the peak of EAE (n = 6). Demyelination of representative brain sections is indicated by loss of blue staining (scale bars indicate 1 mm and 100 μm for lower and higher magnification, respectively), and the total demyelinated area was measured with ImageJ. The results represent at least two independent experiments (A–C). *P < 0.05, **P < 0.005.
Supplemental Figure 4. Cd226−/− iTregs do not display decreased apoptosis. (A) The purity of Tregs before and after magnetic separation was determined by FCM (n = 6). (B) The relative mRNA expression levels of TGF-β in splenic Tregs from WT or Cd226−/− mice during EAE were assessed by qRT-PCR. (C) Annexin V and PI staining of iTregs after polarization from WT and Cd226−/− naïve CD4+ T cells for 3 days (n = 6). The results represent two or three independent experiments (A–C). The numbers in each quadrant show the percentage of the relevant cell population.
Supplemental Table 1. The primers used for qRT-PCR in this study are listed.
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Keywords: CD226, EAE, Tregs, proliferation, suppression, Akt signaling, Erk signaling
Citation: Wang N, Yi H, Fang L, Jin J, Ma Q, Shen Y, Li J, Liang S, Xiong J, Li Z, Zeng H, Jiang F, Jin B and Chen L (2020) CD226 Attenuates Treg Proliferation via Akt and Erk Signaling in an EAE Model. Front. Immunol. 11:1883. doi: 10.3389/fimmu.2020.01883
Received: 10 November 2019; Accepted: 13 July 2020;
Published: 21 August 2020.
Edited by:
Bruno Stankoff, Sorbonne Universités, FranceReviewed by:
Chiara Cordiglieri, National Institute of Molecular Genetics (INGM), ItalyCai Zhang, Shandong University, China
Qing Ge, Peking University, China
Copyright © 2020 Wang, Yi, Fang, Jin, Ma, Shen, Li, Liang, Xiong, Li, Zeng, Jiang, Jin and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Lihua Chen, chenlh@fmmu.edu.cn